Human Phenotype Ontology 
Grandparent Node:
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Abnormal posterior eye segment morphology (HP:0004329)help
Parent Node:
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Abnormal vitreous humor morphology (HP:0004327)help
..Starting node
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Asteroid hyalosis (HP:0030672)help
Term ID: 30672
Name: Asteroid hyalosis
Synonym:
Definition: The presence of small, white vitreous opacities consisting of calcium phosphate and complex, layered lipid deposits.
Comments:
Reference: HP:0030672
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAmyloid deposition in the vitreous humor (HP:0007841) help
..expandBeaded vitreous appearance (HP:0031154) help
..expandMembranous vitreous appearance (HP:0031153) help
..expandOptically empty vitreous (HP:0030663) help
..expandPeripheral vitreous opacities (HP:0007710) help
..expandPosterior vitreous detachment (HP:0001489) help
..expandRemnants of the hyaloid vascular system (HP:0007968) help
..expandVitreoretinopathy (HP:0007773) help
..expandVitreous floaters (HP:0100832) help
..expandVitreous hemorrhage (HP:0007902) help
..expandVitritis (HP:0011531) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030672HP:0030672Asteroid hyalosis0ARL3 CL E G H403694OMIM:618173RETINITIS PIGMENTOSA 83; RP831
HP:0030672HP:0030672Asteroid hyalosis0COL2A1 CL E G H12802200OMIM:132450Epiphyseal dysplasia, multiple, with myopia and conductive deafness.284
HP:0030672HP:0030672Asteroid hyalosis0COL2A1 CL E G H12802200ORPHA:166011Multiple epiphyseal dysplasia, Beighton typeHP:0040283 - Occasional284
HP:0030672HP:0030672Asteroid hyalosis0PRPF8 CL E G H1059417340OMIM:600059Retinitis pigmentosa 1394


Genes (3) :ARL3 COL2A1 PRPF8

Diseases (4) :OMIM:618173 OMIM:132450 ORPHA:166011 OMIM:600059
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.